Publikace
- Multiple (familial) trichoepitheliomas: a clinicopathological and molecular biological study, including CYLD and PTCH gene analysis, of a series of 16 patients2011 | 1. lékařská fakulta, Lékařská fakulta v Plzni
- Recurrent CYLD nonsense mutation associated with a severe, disfiguring phenotype in an African American family with multiple familial trichoepithelioma2011 | 1. lékařská fakulta, Lékařská fakulta v Plzni
- Extra nuchal-type fibroma associated with elastosis, traumatic neuroma, a rare APC gene missense mutation, and a very rare MUTYH gene polymorphism: a case report and review of the literature2011 | 1. lékařská fakulta, Lékařská fakulta v Plzni
- Lymphocyte-rich renal cell carcinoma : an unusual histomorphologic manifestation of a tumor that is not part of Lynch syndrome2011 | 1. lékařská fakulta, Lékařská fakulta v Plzni
- Brooke-Spiegler syndrome: report of 10 patients from 8 families with novel germline mutations2010 | Ústřední knihovna
- Novel insights into the BAP1-inactivated melanocytic tumor2022 | Lékařská fakulta v Plzni
- Primary cutanous desmoplastic melanoma with collagen rosettes and pseudoglandular features2021 | Lékařská fakulta v Plzni
- Extramammary Paget disease of the vulva2021 | Lékařská fakulta v Plzni
- Atypical Non-neoplastic Changes in Anogenital Mammary-like Glands Accompanying Invasive Squamous Cell Carcinoma2021 | Lékařská fakulta v Plzni
- Lichen aureus with pseudolymphomatous infiltrate2021 | Lékařská fakulta v Plzni
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